| 1. |
- Hoshino, Yosuke, et al.
(författare)
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Cryogenian evolution of stigmasteroid biosynthesis
- 2017
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Ingår i: Science Advances. - : AMER ASSOC ADVANCEMENT SCIENCE. - 2375-2548. ; 3:9
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Tidskriftsartikel (refereegranskat)abstract
- Sedimentary hydrocarbon remnants of eukaryotic C-26-C-30 sterols can be used to reconstruct early algal evolution. Enhanced C-29 sterol abundances provide algal cellmembranes a density advantage in large temperature fluctuations. Here, we combined a literature review with new analyses to generate a comprehensive inventory of unambiguously syngenetic steranes in Neoproterozoic rocks. Our results show that the capacity for C-29 24ethyl- sterol biosynthesis emerged in the Cryogenian, that is, between 720 and 635 million years ago during the Neoproterozoic Snowball Earth glaciations, which were an evolutionary stimulant, not a bottleneck. This biochemical innovation heralded the rise of green algae to global dominance of marine ecosystems and highlights the environmental drivers for the evolution of sterol biosynthesis. The Cryogenian emergence of C-29 sterol biosynthesis places benchmark for verifying older sterane signatures and sets a new framework for our understanding of early algal evolution.
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| 2. |
- Brocks, J. J., et al.
(författare)
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Early sponges and toxic protists : possible sources of cryostane, an age diagnostic biomarker antedating Sturtian Snowball Earth
- 2016
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Ingår i: Geobiology. - : Wiley. - 1472-4677 .- 1472-4669. ; 14:2, s. 129-149
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Tidskriftsartikel (refereegranskat)abstract
- The period 800-717million years (Ma) ago, in the lead-up to the Sturtian Snowball glaciation, saw an increase in the diversity of eukaryotic microfossils. To afford an independent and complementary view of this evolutionary period, this study presents the distribution of eukaryotic biomarkers from three pre-Sturtian successions across the supercontinent Rodinia: the ca. 780Ma Kanpa Formation of the Western Australian Officer Basin, the ca. 800-740Ma Visingso Group of Sweden, and the 740Ma Chuar Group in Arizona, USA. The distribution of eukaryotic steranes is remarkably similar in the three successions but distinct from all other known younger and older sterane assemblages. Cholestane was the only conventional structure, while indigenous steranes alkylated in position C-24, such as ergostane, stigmastane, dinosterane and isopropylcholestane, and n-propylcholestane, were not observed. This sterane distribution appears to be age diagnostic for the pre-Sturtian Neoproterozoic. It attests to the distinct evolutionary state of pre-Snowball eukaryotes, pointing to a taxonomic disparity that was still lower than in the Ediacaran (635-541Ma). All three basins also show the presence of a new C-28 sterane that was tentatively identified as 26-methylcholestane, here named cryostane. The only known extant organisms that can methylate sterols in the 26-position are demosponges. This assignment is plausible as molecular clocks place the appearance of the earliest animals into the pre-Sturtian Neoproterozoic. The unusual 26-methylsterol may have protected sponges, but also other eukaryotes, against their own membranolytic toxins. Some protists release lytic toxins to deter predators and kill eukaryotic prey. As conventional membrane sterols can be the site of attack for these toxins, sterols with unusual side-chain modification protect the cell. This interpretation of cryostane supports fossil evidence of predation in the Chuar Group and promotes hypotheses about the proliferation of eukaryophagy in the lead-up to the Cryogenian.
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| 3. |
- Xiao, Shuhai, et al.
(författare)
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Towards an Ediacaran Time Scale : Problems, Protocols, and Prospects
- 2016
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Ingår i: Episodes. - : International Union of Geological Sciences. - 0705-3797 .- 2586-1298. ; 39:4, s. 540-555
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Tidskriftsartikel (refereegranskat)abstract
- The Ediacaran Period follows the Cryogenian Period in the wake of a snowball Earth glaciation and precedes the Cambrian Period with its rising tide of animal radiation. It is also the longest among all stratigraphically defined geological periods, lasting 94 million years (635-541 Ma). Hence, a good Ediacaran time scale is essential, not only to elucidate geological time, but also to provide a temporal context for extreme climatic events and transformative evolutionary transitions. Ediacaran fossils are known from many sections and boreholes around the world, permitting ready age recognition and stratigraphic correlation of Ediacaran strata. However, the Ediacaran fossil record is colored by taphonomic biases that variously affect the preservation of the soft-bodied organisms that dominated Ediacaran marine ecosystems, and the Phanerozoic approach of defining stratigraphic boundaries using the first appearance datum (FAD) of widely distributed, rapidly evolving, easily recognizable, and readily preservable species would have limited success in the Ediacaran System. The subdivision of the Ediacaran System must therefore be founded on a holistic approach integrating biostratigraphic, chemostratigraphic, and geochronometric data for correlation. Series-level subdivision of the Ediacaran System is a challenging task, and alternative models subdividing the Ediacaran System into two or three series can be recognized. Resolving these alternatives critically depends on obtaining further data to constrain the age, duration, and global extent of the Shuram negative delta C-13 excursion, to calibrate and correlate Ediacaran acanthomorph biozones, and to determine the temporal relationship among the Shuram excursion, the Gaskiers glaciation, and Ediacaran acanthomorph biozones. Stage-level subdivisions at the bottom and top of the Ediacaran System, however, are realistic goals in the near future, and we propose that the subdivision of the Ediacaran System should initially aim at the second Ediacaran stage (SES) and the terminal Ediacaran stage (TES) where stratigraphic information is relatively rich and consensus for stratigraphic correlation is emerging. Potential stratigraphic markers for the definition of the SES include the post-glacial radiation of eukaryotes as represented by the first appearance of acanthomorph acritarchs, the termination of the cap carbonate series, or the end of the negative delta C-13 excursion (EN1 = Ediacaran negative excursion 1) associated with the cap carbonate. Terminal Ediacaran strata are well dated and host several taxa of skeletal and tubular fossils that postdate the Shuram negative delta C-13 excursion (or its probable equivalent, EN3 = Ediacaran negative excursion 3) where their stratigraphic relationship can be determined; these biostratigraphic markers may be used to define the TES in a Phanerozoic fashion. Additional Ediacaran stages between the SES and TES can be envisioned. Through collaborative efforts in the Ediacaran community, we hope that the first Precambrian stage will be established in the near future to facilitate a better understanding of the geological aftermath of snowball Earth, the redox history of global oceans, the early evolution of multicellular life, and the evolutionary fuse of the Cambrian explosion.
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